prednisone

Generic: prednisone

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prednisone
Generic Name prednisone
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prednisone 20 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-430
Product ID 72189-430_49eeb073-7434-0657-e063-6394a90ab0a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208412
Listing Expiration 2027-12-31
Marketing Start 2023-03-03

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189430
Hyphenated Format 72189-430

Supplemental Identifiers

RxCUI
312615
UNII
VB0R961HZT
NUI
N0000175576 N0000175450

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prednisone (source: ndc)
Generic Name prednisone (source: ndc)
Application Number ANDA208412 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 5 TABLET in 1 BOTTLE (72189-430-05)
  • 10 TABLET in 1 BOTTLE (72189-430-10)
  • 15 TABLET in 1 BOTTLE (72189-430-15)
  • 20 TABLET in 1 BOTTLE (72189-430-20)
  • 21 TABLET in 1 BOTTLE (72189-430-21)
  • 30 TABLET in 1 BOTTLE (72189-430-30)
source: ndc

Packages (6)

72189-430-05 5 TABLET in 1 BOTTLE (72189-430-05) 72189-430-10 10 TABLET in 1 BOTTLE (72189-430-10) 72189-430-15 15 TABLET in 1 BOTTLE (72189-430-15) 72189-430-20 20 TABLET in 1 BOTTLE (72189-430-20) 72189-430-21 21 TABLET in 1 BOTTLE (72189-430-21) 72189-430-30 30 TABLET in 1 BOTTLE (72189-430-30)

Ingredients (1)

prednisone (20 mg/1)

Linked Drug Pages (1)

Prednisone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49eeb073-7434-0657-e063-6394a90ab0a6", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["312615"], "spl_set_id": ["f6051257-2144-4487-e053-2995a90a973b"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "5 TABLET in 1 BOTTLE (72189-430-05)", "package_ndc": "72189-430-05", "marketing_start_date": "20230303"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (72189-430-10)", "package_ndc": "72189-430-10", "marketing_start_date": "20230303"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (72189-430-15)", "package_ndc": "72189-430-15", "marketing_start_date": "20230303"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-430-20)", "package_ndc": "72189-430-20", "marketing_start_date": "20230303"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-430-21)", "package_ndc": "72189-430-21", "marketing_start_date": "20230303"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-430-30)", "package_ndc": "72189-430-30", "marketing_start_date": "20230303"}], "brand_name": "Prednisone", "product_id": "72189-430_49eeb073-7434-0657-e063-6394a90ab0a6", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-430", "generic_name": "Prednisone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "20 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20230303", "listing_expiration_date": "20271231"}